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ICON

Warsaw, Poland
Clinical trial site visits
Protocol compliance monitoring
Data integrity assurance
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • As a Clinical Research Associate II, you will conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and patient safety.
  • ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • clinical trial site visits
  • protocol compliance monitoring
  • data integrity assurance
  • patient safety oversight
  • clinical data query resolution
  • international and domestic travel
  • valid driver’s license

Nice-to-have

  • collaborative team environment
  • strong organizational skills
  • effective communication skills
  • attention to detail
  • fast-paced work adaptability
  • inclusive workplace culture

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years Clinical Research Associate experience
  • In-depth knowledge of clinical trial regulations and ICH-GCP guidelines
  • Ability to travel at least 60%
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter